Address
SalaryRole and responsibilities
Reviewing technical, promotional and medical materials from a range of pharmaceutical companies/ agencies (medical accuracy and code compliance).
Taking responsibility of Quality Control of other reviewers work once agreed with Business Unit Director.
Covering absences for WIP lead or Team Lead, as directed.
Ensuring up-to-date knowledge regarding a variety of therapeutic areas and client products; attending relevant training.
Attend monthly mentorship sessions held by Team Lead on topics of interest
Maintaining up-to-date knowledge of Codes of practice (ABPI, IPHA, EFPIA, PhRMA) including any updates.
Work may be escalated for checks (“TPOE”) by Team Lead / BUD
Attending client meetings to support Team Leader and/ or Business Unit Director for professional development purposes.
May be required to lead a job bag workstream (WIP)
Good timekeeping.
Regular meetings with line manager and appropriate escalation of any issues.
Key requirements for role
Biomedical MSc, Biomedical PhD, Medical or Pharmacy degree
Minimum 1 year experience of copy reviewing scientific materials
Fluent in Spanish and English language
Excellent eye for detail
Flexible approach to work
Team player
Exceptional communication skills
Ability to work under high pressure
Experience on an approval system like Veeva Promomats is desirable
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
